Senior Clinical Research Coordinator

Kaiser Permanente; Los Angeles (CA); On-site; USD 90,000 - 120,000; Full time

Job summary

Kaiser Permanente is seeking a detailed and collaborative clinical research professional to support data collection, documentation, and regulatory submissions for trials. You will work with investigators and staff to ensure timely, compliant study conduct and effective communication across departments.

Responsibilities include drafting protocol materials, supporting IRB submissions, and helping implement study quality measures while maintaining data integrity and participant safety.

Qualifications

• Bachelor's degree required or higher in science/health fields.
• Two years of clinical research experience or five years for non-traditional backgrounds.
• Experience with regulatory submissions and IRB processes preferred.

Responsibilities

• Drafts and submits clinical trial applications to regulatory bodies (IRB/KP policies).
• Collects and documents data for clinical trials and supports lab operations as needed.
• Develops education materials for staff and participants on protocols and timelines.
• Maintains compliance with federal, state, and local regulations and KP policies.

Skills

Attention to Detail

Communication

Project Management

Data Quality

Clinical Research

Problem Solving

Adaptability

Autonomy

Teamwork

Integrity

Education

Bachelor's degree in Science, Public Health, Health Care Administration, or related field

Tools

Laboratory Equipment

Job description

Kaiser Permanente is seeking a detailed and collaborative clinical research professional to support data collection, documentation, and regulatory submissions for trials. You will work with investigators and staff to ensure timely, compliant study conduct and effective communication across departments.

Responsibilities include drafting protocol materials, supporting IRB submissions, and helping implement study quality measures while maintaining data integrity and participant safety.